AA-1110 ANALOG ABUTMENT— 510(k) K903042

Name: FDA 510(k) clearance K903042
Creator: U.S. Food and Drug Administration
Published: 1990-11-13

Substantially Equivalent

Minimatic Implant Technology

FDA 510(k) clearance K903042 for AA-1110 ANALOG ABUTMENT, Substantially Equivalent on 1990-11-13. Applicant: Minimatic Implant Technology. Device class: 2.

Clearance details

Applicant: Minimatic Implant Technology
Product code: Code DZE
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 1990-07-11
Decision date: 1990-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deerfield Beach, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DZE

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K260463 — ZEROS Dental Implant System2026-08-19
K251188 — UNIQA® Dental Implants System2026-06-25
K250806 — Dental Implant System2026-06-18
K251232 — MegaGen Zygoma Dental Implant System2026-06-18
K260006 — INOSS System2026-06-17

More clearances from Minimatic Implant Technology

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K911776 — DPI-1106 IMPLANT, MODIFICATION1992-01-15
K903515 — HH-1119 HEALING HEAD1991-07-04
K911112 — DEVICE PART NUMBERS: - 1400 SERIES1991-06-10
K904707 — BC 1208 IMPLANT, THREADED EXTERNAL HEX1991-04-29
K905039 — IMPLANT, THREADED EXTERNAL HEX, TAPERED SHOULDER1991-04-29

Adverse events under product code DZE

product code DZE

Death: 28
Injury: 3,367,041
Malfunction: 19,958
Other: 13
Total: 3,387,040

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.